Status:

RECRUITING

Asleep Fiberoptic vs Direct Laryngoscopy Effect on Hemodynamic Stability Using Opioid Free Anesthesia Induction

Lead Sponsor:

American University of Beirut Medical Center

Conditions:

Analgesics, Opioid

Anesthesia, General

Eligibility:

All Genders

18-55 years

Phase:

NA

Brief Summary

The goal of this clinical trial is to compare blood pressure and heart rate between the fiberoptic and direct oral intubation using opioid free anesthesia induction. Secondary objectives include compa...

Detailed Description

Background: Intubation has always been linked to a transient increase in blood pressure and heart rate that could be deleterious in elderly and hemodynamically unstable patients. Fiberoptic intubation...

Eligibility Criteria

Inclusion

  • ASA (American Society of Anesthesiologists) physical status I and II
  • Range age of 18-55 years' old
  • Scheduled for elective surgery under general anesthesia.

Exclusion

  • History of cardiovascular diseases.
  • History of lung disease.
  • Hypertensive patient (BP\> 140/90)
  • Patient taking medications that affect blood pressure and heart rate
  • Morbid obesity (BMI \>30)
  • Severe GERD
  • Predicted difficult airway (Short TMD \<6 cm, Upper li bite test grade III, Mallampati score
  • \>III)
  • Neck instability
  • Patient planned to receive rapid sequence intubation
  • Patient refusal to participate
  • History of difficult intubation/ ventilation

Key Trial Info

Start Date :

September 11 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2026

Estimated Enrollment :

90 Patients enrolled

Trial Details

Trial ID

NCT06487988

Start Date

September 11 2024

End Date

January 1 2026

Last Update

December 19 2025

Active Locations (1)

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1

Christian Rouphael

Beirut, Lebanon